Search results for OTX2

38 hits were found for OTX2

# Family MCID Name MIFTS Score
1
c MCR252 Microphthalmia, Syndromic 5 27 13.537
2
MCR013 Microphthalmia 60 5.341
3
P MDL005 Medulloblastoma 77 4.926
4
PTT043 Pituitary Hormone Deficiency, Combined, 6 19 4.801
5
AGN012 Agnathia-Otocephaly Complex 53 4.352
6
CMB021 Combined Pituitary Hormone Deficiency 37 3.965
7
P ANR002 Aniridia 64 3.847
8
HMF006 Hemifacial Microsomia 55 3.847
9
PTT001 Pituitary Hypoplasia 31 3.810
10
OTX001 Otx2-Related Combined Pituitary Hormone Deficiency 11 3.411
11
P ANP022 Anophthalmia/microphthalmia 31 3.378
12
DYS038 Dysgnathia Complex 17 3.378
13
ISL003 Isolated Growth Hormone Deficiency 52 3.341
14
P BRN006 Branchiootorenal Syndrome 40 3.341
15
CMB062 Combined Pituitary Hormone Deficiencies, Genetic Forms 29 3.341
16
BTT011 Butterfly-Shaped Pigment Dystrophy 24 3.341
17
RTN139 Retinal Dystrophy, Early-Onset, and Pituitary Dysfunction 3 3.341
18
CHR103 Charge Syndrome 62 3.300
19
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 57 3.300
20
APH010 Aphakia, Congenital Primary 44 3.300
21
INF039 Infratentorial Cancer 42 3.300
22
FRY006 Fryns Microphthalmia Syndrome 36 3.300
23
MDL003 Medullomyoblastoma 35 3.300
24
VLP001 Valproate Embryopathy, Susceptibility to 35 3.300
25
RTN023 Retinitis 50 0.155
26
NRN002 Neuronitis 41 0.155
27
GRW007 Growth Hormone Deficiency 50 0.134
28
P RTN024 Retinoblastoma 74 0.110
29
c MCR263 Microphthalmia, Syndromic 1 34 0.110
30
P BPL003 Bipolar Disorder 62 0.078
31
EMB004 Embryonal Carcinoma 57 0.078
32
HYP080 Hypogonadism 53 0.078
33
P INT063 Intellectual Disability 49 0.078
34
DYS018 Dysostosis 44 0.078
35
PTT041 Pituitary Stalk Interruption Syndrome 42 0.078
36
HYP064 Hypogonadotropism 37 0.078
37
SPT019 Septo-Optic Dysplasia Spectrum 32 0.078
38
PTT045 Pituitary Hormone Deficiency, Combined, 1 30 0.078
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